Lilly

healthcare

Supervisor-IDAPVaultOperations

$0–0k Indianapolis, Indiana, United States FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid+ candidates.

The Brief

“Supervisor - IDAP Vault Operations at Lilly. Skills: shift leadership, daily operations, safety, compliance, operator development, resource scheduling, production issue resolution. shift leadership for the Vault Device Assembly process team. daily operations”

What You'll Achieve.

Delivering quality performance for the shift in accordance with established procedures; driving improvement in these areas

Industry & Context.

healthcare
Problems you'll solve

helping resolve any production issues in real-time; Ability to identify gaps proactively

Eligibility Requirements

12-hour shift position on a 3-2-2-3 schedule on potentially A (day) or (night) shift, Overtime may be required, Some roles require ability to work with controlled substances – background check is required for those instances

What They're Looking For.

Must Have

High School Diploma or equivalent, safety and quality mindset, Demonstrated leadership abilities in holding accountability, setting and maintaining high expectations, developing team for operational excellence, computer skills including Excel, Word, Outlook, etc, Ability to communicate to various levels of the organization (operators, maintenance, engineers, managers, etc), Process/Continuous improvement mindset, Manufacturing experience with knowledge of cGMP requirements, Ability to identify gaps proactively and work cross-functionally to mitigate and strengthen team, Qualified candidates must be legally authorized to be employed in the United States

Nice to Have

Previous supervisor/leadership experience, Ability to navigate SAP, EWM, MES, VEEVA systems, Proficiency in Microsoft Office programs, Device Assembly or Packaging Operations experience

What You'll Do.

shift leadership for the Vault Device Assembly process team

ensuring compliance with all policies/procedures/training

development of operators

ensuring resources are scheduled accordingly per the production plan

helping resolve any production issues in real-time

Demonstrating and delivering a safety culture for the shift

Delivering quality performance for the shift in accordance with established procedures

Ensuring the shift follows all cGMP requirements and ALCOA+ principles

Staffing of the device assembly lines with trained/qualified operators

and coaching operators

Identifying opportunities for continuous improvement in safety

quality and productivity

and driving improvement in these areas

Communicating with area leadership and support personnel on safety

and operational issues

Investigating and documenting safety/quality incidents that occur in the area

Lead HSE investigations with your team

Strict adherence to IDAP and Lilly employee policies and expectations

How You'll Work.

Team & Collaboration

cross-functionally to mitigate and strengthen team; Communicating with area leadership and support personnel on safety, quality, engineering, and operational issues; Lead HSE investigations with your team

Communication Scope

Ability to communicate to various levels of the organization (operators, maintenance, engineers, managers, etc)

Full Job Description

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. **Position Brand Description:** The Supervisor – IDAP Vault Operations provides shift leadership for the Vault Device Assembly process team. The Leader is responsible for daily operations including: safety of the people, ensuring compliance with all policies/procedures/training, development of operators, ensuring resources are scheduled accordingly per the production plan, and helping resolve any production issues in real-time. This is a 12-hour shift position on a 3-2-2-3 schedule on potentially A (day) or B (night) shift. **Responsibilities:** * Demonstrating and delivering a strong safety culture for the shift * Delivering strong quality performance for the shift in accordance with established procedures * Ensuring the shift follows all cGMP requirements and ALCOA+ principles * Staffing of the device assembly lines with trained/qualified operators * Supervising, developing, and coaching operators * Identifying opportunities for continuous improvement in safety, quality and productivity, and driving improvement in these areas * Communicating with area leadership and support personnel on safety, quality, engineering, and operational issues * Investigating and documenting safety/quality incidents that occur in the area * Lead HSE investigations with your team * Strict adherence to IDAP and Lilly employee policies and expectations **Basic Qualifications:** * High School Diploma or equivalent. * Strong safety and quality mindset

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